MEDICAL AFFAIRS AND CLINICAL jobs in CAMBRIDGESHIRE, United Kingdom

Job Title Medical Affairs Specialist Job Description As a Medical Affairs Specialist, you will help to develop the... Medical Office within HPM, contribute with clinical context in the whole lifecycle of our solutions and products. In...

, you will be responsible for acting as one of the EU Regulatory leads for Kite's existing commercial and/or clinical programs. Your duties... hoc or special projects aimed at continuously improving or advancing Regulatory Affairs capabilities. In your new role...

Company Description Bicycle Therapeutics is a clinical-stage biopharmaceutical company developing a novel class... Immune Cell Agonist® (Bicycle TICA®) targeting Nectin-4 and agonizing CD137, in company-sponsored clinical trials...

Proclinical is seeking a Regulatory Affairs Manager. This role is pivotal in providing country-specific regulatory... of marketing authorisations, clinical trial application submissions and regulatory support for commercial activities...

, contribute and ensure the accurate preparation of high-quality regulatory documents needed to support clinical trials and medical...An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, UK/IE...

. Job Description As a Director, Global Regulatory Affairs, Precision Medicine you will develop and execute Precision Medicine regulatory strategies... President, Global Regulatory Affairs Oncology and Precision Medicine, and collaborate with the biomarker team and global...

innovative medical devices, which we use in clinical trials to collect a biobank of mucus-based biospecimens. This biobank... provides clinical material for our research and development streams to assist with diagnostic development. Our primary...

conjunction with Clinical Development Program Directors (CDPDs), Medical Dev. Directors (MDDs), and other Ipsen team members... with Medical Dev. Director (MDD) and other relevant Ipsen team members Lead clinical project processes Lead cross-functional...

Medical Affairs function Assist in scientific advisory boards, conference activities, external collaborations...Company Description Bicycle Therapeutics is a clinical-stage biopharmaceutical company developing a novel class...

Affairs) who can support Clinical Operations at various steps (site qualification, site recruitment) Ensure the monitoring...Title: Clinical Monitoring Lead Company: Ipsen Bioscience, Inc. Job Description: Clinical Monitoring Lead (CML...

Affairs) who can support Clinical Operations at various steps (site qualification, site recruitment) Ensure the monitoring...Title: Clinical Monitoring Lead Company: Ipsen Bioscience, Inc. Job Description: Clinical Monitoring Lead (CML...

Job Purpose The Senior Manager, Medical & Regulatory Writing will be an integral part of MoonLake’s Clinical.... Key Accountabilities: Lead scientific contribution to the development of medical, regulatory and clinical documents...

Company Description Bicycle Therapeutics is a clinical-stage biopharmaceutical company developing a novel class... Immune Cell Agonist® (Bicycle TICA®) targeting Nectin-4 and agonizing CD137, in company-sponsored clinical trials...

Affairs will report to the Sr. Director and have accountability for review and approval of promotional and medical... and strong collaboration with Commercial Marketing, Medical Affairs, PRC/MRC Coordinators, Legal Affairs, Regulatory Affairs Strategy, Labeling...

with Commercial Marketing, Medical Affairs, PRC/MRC Coordinators, Legal Affairs, Regulatory Affairs Strategy, Labeling Operations.... Job Description: Associate Director, Commercial Regulatory Affairs Position Summary The Associate Director, Commercial Regulatory Affairs...

in the industry. Experience in one or more of the following Clinical Development functions in support of IT – Medical... Affairs, Regulatory Affairs, Global Patient Safety, Clinical Operations, BioStats & Data Management, Clinical Quality...

Job Purpose As a Senior Manager, Regulatory Affairs CMC, you are an integral part of MoonLake’s Clinical Development... team responsible for the development, execution and tracking of regulatory CMC and medical device activities...